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EIPG Newsletter
Regulatory
Regulatory
EMA opened a consultation on the use of patient registries for...
Giuliana Miglierini
-
11 December 2018
0
The use of real world data for R&D of pharmaceuticals
Giuliana Miglierini
-
21 November 2018
0
Brexit: EU Commission warns on possible issues regarding clinical trials
Giuliana Miglierini
-
23 October 2018
0
Regulators launched activities to prepare for the Brexit
Giuliana Miglierini
-
20 September 2018
0
Pharma companies are not yet ready for the Brexit
Giuliana Miglierini
-
2 August 2018
0
3D printing, a disruptive technology still lacking regulatory guidance in the...
Giuliana Miglierini
-
19 July 2018
0
Αccelerated assessment of PRIority Medicines (the PRIME programme)
Giuliana Miglierini
-
19 June 2018
0
Redistribution of the UK centrally authorised product portfolio
Giuliana Miglierini
-
28 May 2018
0
Towards the harmonisation of clinical evaluation of medical devices
Giuliana Miglierini
-
19 April 2018
0
An update on orphan medicines and rare diseases
Giuliana Miglierini
-
20 March 2018
0
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